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- B9b0077666adae1176701415ad80f3f9b hasDbXref "Orphanet:1667" @default.
- B9b0077666adae1176701415ad80f3f9b type Axiom @default.
- B9b0077666adae1176701415ad80f3f9b annotatedProperty IAO_0000115 @default.
- B9b0077666adae1176701415ad80f3f9b annotatedSource MONDO_0009192 @default.
- B9b0077666adae1176701415ad80f3f9b annotatedTarget "Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure." @default.